Single-Use Biopsy Forceps

GUDID 06936937712997

Jiangsu Grit Medical Technology Co., Ltd.

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• Primary Device ID: 06936937712997
• NIH Device Record Key: d5c3e732-7677-448f-8528-cc514b2ded07
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Single-Use Biopsy Forceps
• Version Model Number: RP-U-P16F
• Company DUNS: 554536935
• Company Name: Jiangsu Grit Medical Technology Co., Ltd.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: false
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: true
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	06936937712997 [Primary]

FDA Product Code

• FCL: Forceps, Biopsy, Non-Electric

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-12-21
• Device Publish Date: 2023-12-13

On-Brand Devices [Single-Use Biopsy Forceps]

• 06936937713307: RP-U-P17F
• 06936937712997: RP-U-P16F